ENST00000480188.2:n.1396A=
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|
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ENST00000696279.1:c.4682A=
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|
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ENST00000696280.1:n.4451A=
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|
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ENST00000696281.1:c.4380A=
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ENSP00000512521.1:p.Gln1460=
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ENST00000697921.1:n.3240A=
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|
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ENST00000697922.1:c.*4352A=
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ENSP00000513478.1:n.*4352A=
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ENST00000697923.1:n.4807A=
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|
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ENST00000223642.3:c.4362A=
MANE Select
|
ENSP00000223642.1:p.Gln1454=
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|
ENST00000223642.2:c.4362A=
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ENSP00000223642.1:p.Gln1454=
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|
NM_001735.2:c.4362A= , LRG_28t1:c.4362A=
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NP_001726.2:p.Gln1454=
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|
XM_011518980.1:c.4377A=
|
XP_011517282.1:p.Gln1459=
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|
NM_001317163.1:c.4380A=
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NP_001304092.1:p.Gln1460=
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|
NM_001317163.2:c.4380A=
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NP_001304092.1:p.Gln1460=
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|
NM_001735.3:c.4362A=
MANE Select
|
NP_001726.2:p.Gln1454=
|
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